BEUDAMED
    176 results · 30ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    HEPATIC ENZYMES ON ABX PENTRA 400 CLINICAL CHEMISTRY ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Vivid Etch 40% refill

    FDA UDI
    PEARSON DENTAL SUPPLIES, INC.·D724Z0603180·60G

    Mini-Mono®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70603181·Mini-Mono-Brackets Roth 'N' .022" 9° 100 Bracke...

    PRIMA OXYGEN MONITOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BIONOSTICS GLUCOSE QUALITY CONTROL SOLUTION FOR USE WITH THE FASTTAKE COMPACT BLOOD GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    BD PHOENIX PMIC110

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·October 19, 2021

    BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·August 23, 2021

    BD PHOENIX PANEL PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 10, 2023

    BD PHOENIX PANEL PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 10, 2023

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·September 2, 2025

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·September 2, 2025

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·April 15, 2024

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 23, 2024

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 26, 2024

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 26, 2024

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·April 11, 2013

    ONE TOUCH ULTRAMINI METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·June 13, 2008

    MINI TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·April 15, 2011

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 27, 2024

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·August 26, 2024